Canonical Allele Identifier: PA231622
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 47639
ClinVar RCV Id: RCV000040908 RCV000246329 RCV000769857 RCV000713950 RCV001131492 RCV001131493 RCV001134484 RCV000852780 RCV001131495 RCV001079468 RCV001131494 RCV002227931
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_596869.4:p.Val31321Ile
CA231620
NM_133378.4:c.93961G>A